Food and Drug Regulations

Version of section C.03.207 from 2018-04-04 to 2018-06-12:


 Every component shall be labelled to show

  • (a) adequate identification of the component and an adequate description of its function;

  • (b) where applicable, a quantitative list of its ingredients or a reference to the label of the kit that shows such information;

  • (c) the name of the distributor referred to in paragraph C.01A.003(b);

  • (d) the lot number;

  • (e) a statement of any special storage requirements with respect to temperature and light;

  • (f) the date after which the component is not recommended for use, the name of the month being written in full or designated by letter abbreviation; and

  • (g) adequate directions for use or a reference to the accompanying package insert that shows such directions.

  • SOR/79-236, s. 4;
  • SOR/97-12, s. 58;
  • SOR/2018-69, s. 23(F).
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